Suppressive effects of aryl-hydrocarbon receptor repressor on adipocyte differentiation in 3T3-L1 cells

被引:14
作者
Ishihara, Yasuhiro [1 ,2 ]
Tsuji, Mayumi [1 ,3 ]
Vogel, Christoph F. A. [1 ,4 ]
机构
[1] Univ Calif Davis, Ctr Hlth & Environm, Davis, CA 95616 USA
[2] Hiroshima Univ, Grad Sch Integrated Arts & Sci, 1-7-1 Kagamiyama, Higashihiroshima, Hiroshima 7398521, Japan
[3] Univ Occupat & Environm Hlth, Dept Environm Hlth, Fukuoka 8078555, Japan
[4] Univ Calif Davis, Dept Environm Toxicol, Davis, CA 95616 USA
基金
美国国家卫生研究院;
关键词
AHR REPRESSOR; PPAR-GAMMA; ADIPOGENESIS; KINASE; INFLAMMATION; 2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN; FIBROBLASTS; ACTIVATION; EXPRESSION; PATHWAY;
D O I
10.1016/j.abb.2018.01.018
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The aryl-hydrocarbon receptor repressor (AhRR) negatively regulates aryl-hydrocarbon receptor (AhR) signaling via its inhibitory transactivation. AhR is well known to suppress adipocyte differentiation, but the function of AhRR during adipogenesis is unclear. The purpose of this study was to investigate the role of AhRR in adipocyte differentiation using 3T3-L1 cells. During the early phase of differentiation, AhRR expression was transiently induced, but throughout the entire differentiation process, low levels of AhR expression were maintained. AhRR knockdown significantly increased not only glycerol-3-phosphate dehydrogenase (GPDH) activity but also lipid accumulation inside the cells. AhRR overexpression clearly reduced GPDH activity and lipid accumulation, indicating that AhRR upregulation during the early stage of adipogenesis suppresses adipocyte differentiation. Since AhRR knockdown increases the expression and activity of peroxisome proliferator-activated receptor gamma (PPAR gamma), AhRR negatively regulates PPAR gamma during adipogenesis. In summary, similar to AhR, AhRR acts as an inhibitor of adipocyte differentiation. In addition to controlling the negative feedback loop of AhR, AhRR might be involved in other functions, especially in adipocyte differentiation processes.
引用
收藏
页码:75 / 80
页数:6
相关论文
共 30 条
[1]  
Alexander DL, 1998, J CELL SCI, V111, P3311
[2]   The mammalian aryl hydrocarbon (Ah) receptor: from mediator of dioxin toxicity toward physiological functions in skin and liver [J].
Bock, Karl Walter ;
Koehle, Christoph .
BIOLOGICAL CHEMISTRY, 2009, 390 (12) :1225-1235
[3]   Balancing intestinal and systemic inflammation through cell type-specific expression of the aryl hydrocarbon receptor repressor [J].
Brandstaetter, Olga ;
Schanz, Oliver ;
Vorac, Julia ;
Koenig, Jessica ;
Mori, Tetsushi ;
Maruyama, Toru ;
Korkowski, Markus ;
Haarmann-Stemmann, Thomas ;
von Smolinski, Dorthe ;
Schultze, Joachim L. ;
Abel, Josef ;
Esser, Charlotte ;
Takeyama, Haruko ;
Weighardt, Heike ;
Foerster, Irmgard .
SCIENTIFIC REPORTS, 2016, 6
[4]   Mitogen-activated protein kinase activation is not necessary for, but antagonizes, 3T3-L1 adipocytic differentiation [J].
deMora, JF ;
Porras, A ;
Ahn, N ;
Santos, E .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (10) :6068-6075
[5]   Specific inhibitors of p38 mitogen-activated protein kinase block 3T3-L1 adipogenesis [J].
Engelman, JA ;
Lisanti, MP ;
Scherer, PE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (48) :32111-32120
[6]   Beta-Mecaptoethanol Suppresses Inflammation and Induces Adipogenic Differentiation in 3T3-F442A Murine Preadipocytes [J].
Guo, Wen ;
Li, Yahui ;
Liang, Wentao ;
Wong, Siu ;
Apovian, Caroline ;
Kirkland, James L. ;
Corkey, Barbara E. .
PLOS ONE, 2012, 7 (07)
[7]   Regulation of constitutive and inducible AHR signaling: Complex interactions involving the AHR repressor [J].
Hahn, Mark E. ;
Allan, Lenka L. ;
Sherr, David H. .
BIOCHEMICAL PHARMACOLOGY, 2009, 77 (04) :485-497
[8]   A role for C/EBPβ in regulating peroxisome proliferator-activated receptor γ activity during adipogenesis in 3T3-L1 preadipocytes [J].
Hamm, JK ;
Park, BH ;
Farmer, SR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (21) :18464-18471
[9]   THE ARYL-HYDROCARBON RECEPTOR COMPLEX [J].
HANKINSON, O .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1995, 35 :307-340
[10]   Inducibility of cytochrome P450 1A1 and chemical carcinogenesis by benzo[a]pyrene in AhR repressor-deficient mice [J].
Hosoya, Tomonori ;
Harada, Nobuhiko ;
Mimura, Junsei ;
Motohashi, Hozumi ;
Takahashi, Satoru ;
Nakajima, Osamu ;
Morita, Masanobu ;
Kawauchi, Shimako ;
Yamamoto, Masayuki ;
Fujii-Kuriyama, Yoshiaki .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2008, 365 (03) :562-567